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Raspberry ketone

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Identification
Molecular formula
C10H12O2
CAS number
5471-51-2
IUPAC name
4-(4-hydroxy-3-methoxy-phenyl)butan-2-one
State
State

At room temperature, raspberry ketone is a solid.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
140.00
Boiling point (Kelvin)
413.15
General information
Molecular weight
164.20g/mol
Molar mass
164.2040g/mol
Density
1.0340g/cm3
Appearence

Raspberry ketone is a crystalline solid that is typically white in appearance. It has a characteristic fruity aroma reminiscent of raspberries.

Comment on solubility

Solubility of 4-(4-hydroxy-3-methoxy-phenyl)butan-2-one

The compound 4-(4-hydroxy-3-methoxy-phenyl)butan-2-one exhibits intriguing solubility properties that are influenced by its molecular structure.

Key observations regarding its solubility include:

  • Solvent Polarity: This compound is likely to be more soluble in polar solvents such as methanol, ethanol, and water due to the presence of hydroxyl groups which can engage in hydrogen bonding.
  • Hydrophobic Regions: The methoxy group contributes to the hydrophobic character, which may slightly limit solubility in purely polar solvents, but enhances compatibility with organic solvents like chloroform or acetone.
  • Temperature Dependence: Like many organic compounds, its solubility can be expected to increase with temperature, making it more feasible for dissolution at elevated temperatures.

In general, the solubility of 4-(4-hydroxy-3-methoxy-phenyl)butan-2-one can be summarized as moderate in polar solvents but achieving better dissolution in less polar organic solvents. Such characteristics make it an interesting compound for various applications, depending on the solvent system employed. As noted in chemical literature, "solubility is a critical factor that dictates the utility of a compound in practical applications."

Interesting facts

Interesting Facts about 4-(4-hydroxy-3-methoxy-phenyl)butan-2-one

4-(4-hydroxy-3-methoxy-phenyl)butan-2-one, commonly referred to as a derivative of the phenolic compound, exhibits a fascinating array of properties and applications in various fields of science. Here are some interesting insights into this compound:

  • Natural Occurrence: This compound can be derived from natural sources such as plants, and it is often linked to medicinal properties.
  • Antioxidant Properties: Studies have shown that derivatives of this compound demonstrate significant antioxidant activity, which can help in combating oxidative stress in biological systems.
  • Pharmaceutical Potential: Due to its structural characteristics, it is being researched for its potential use in developing drugs, especially in combating diseases related to oxidative damage.
  • Flavor and Fragrance: Compounds similar to 4-(4-hydroxy-3-methoxy-phenyl)butan-2-one are often used in the flavoring and fragrance industry, providing desirable aromatic properties.
  • Research Applications: In the laboratory, this compound serves as a valuable reagent in organic synthesis, playing a role in producing complex organic molecules.

A notable quote from a recent study highlights its potential: "The exploration of phenolic compounds opens a new frontier in health and environmental sciences."
This statement emphasizes the relevance of phenolic derivatives like 4-(4-hydroxy-3-methoxy-phenyl)butan-2-one across several scientific domains.

In conclusion, as our understanding of compounds like 4-(4-hydroxy-3-methoxy-phenyl)butan-2-one expands, so does the potential for innovative applications in health, pharmaceuticals, and beyond.

Synonyms
ZINGERONE
Vanillylacetone
122-48-5
Zingiberone
4-(4-Hydroxy-3-methoxyphenyl)-2-butanone
4-(4-Hydroxy-3-methoxyphenyl)butan-2-one
Zingherone
Gingerone
Vanillyl acetone
2-Butanone, 4-(4-hydroxy-3-methoxyphenyl)-
4-Hydroxy-3-methoxybenzylacetone
[0]-Paradol
(4-Hydroxy-3-methoxyphenyl)ethyl methyl ketone
(0)-Paradol
3-Methoxy-4-hydroxybenzylacetone
4-(3-Methoxy-4-hydroxyphenyl)-2-butanone
FEMA No. 3124
2-(4-Hydroxy-3-methoxyphenyl)ethyl methyl ketone
DTXSID8047420
CHEBI:68657
NSC-15335
4MMW850892
DTXCID6027420
0 paradol
RefChem:196097
204-548-3
NSC 15335
MFCD00048232
UNII-4MMW850892
Vanillylacetone;Gingerone
CHEMBL25894
4-(4-hydroxy-3-methoxy-phenyl)-butan-2-one
3-Methoxy-4-hydroxy-benzylacetone
(O)-Paradol
CCRIS 2036
HSDB 1064
EINECS 204-548-3
BRN 2051099
vanillylaceton
Zincbacitracin
AI3-31837
[0]Paradol
Zingerone (Standard)
ZINGERONE [FCC]
ZINGERONE [MI]
ZINGERONE [FHFI]
ZINGERONE [HSDB]
4-(4-hydroxy-3-methoxy-phenyl)butan-2-one
4-08-00-01866 (Beilstein Handbook Reference)
SCHEMBL119051
orb1300526
Vanillylacetone, >=96%, FG
VANILLYLACETON [WHO-DD]
SCHEMBL29378477
FEMA 3124
4-(4-hydroxy-3-methoxyphenyl)-
HMS3651E22
MSK40217
NSC15335
Tox21_302493
BDBM50304073
HY-14621R
s2371
SBB071427
STL564783
AKOS009462778
CCG-208511
DB15589
FV05929
Vanillylacetone, >=98%, natural, FG
Zingerone, analytical reference material
NCGC00256663-01
AC-34331
AS-65368
CAS-122-48-5
HY-14621
ST092341
SY017980
4(4-Hydroxy-3-methoxyphenyl)-2-butanone
4-(3-methoxy-4-hydroxyphenyl)butan-2-one
DB-003808
CS-0003480
H1314
NS00013332
SW219618-1
C17497
EN300-1721864
F464499
SR-05000013705
Q1064625
SR-05000013705-1
BRD-K33510429-001-02-3
BRD-K33510429-001-03-1
4-(4-Hydroxy-3-methoxyphenyl)-2-butanone, 9CI, 8CI
Z1255442373
3-Methoxy-4-hydroxybenzylacetone;Zingerone;4-(3-methoxy-4-hydroxyphenyl)-2-butanone
InChI=1/C11H14O3/c1-8(12)3-4-9-5-6-10(13)11(7-9)14-2/h5-7,13H,3-4H2,1-2H